A series of diaryl amines, ethers and thioethers were synthesized under microwave irradiation efficiently at presence of KF/Al2O3 in 83%-96% yields without any solvent. The salient characters of this method lie in short reaction time, high yields, general applicability to substrates and simple workup procedure. At the same time, their antifungal biological activities against six phytopathogen were evaluated. Most of the compounds (3b, 3c, 3g-o) are more potent than thiophannate-methyl against to Magnaporthe oryzae. This implies that diaryl amine or ether moiety may be helpful in finding a fungicide against Magnaporthe oryzae.
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http://dx.doi.org/10.3390/ijms140918850 | DOI Listing |
ACS Omega
December 2024
Key Laboratory of Chemical Biology of Hebei Province, College of Chemistry and Material Science, Hebei University, Baoding, Hebei 071002, P. R. China.
HCl-catalyzed -glycosylation was described herein for the convenient preparation of -heteroaryl -glycosides and polyhydroxylated alkanes with diaryl groups using hetereoaryl amines and unprotected sugars as starting materials. The reaction temperature and the amounts of aryl amines and HCl had significant effects on reactions. The method provided a highly efficient and environmentally friendly route for constructing -glycosides at low cost.
View Article and Find Full Text PDFPhotochem Photobiol Sci
December 2024
PhotoGreen Lab, Department of Chemistry, University of Pavia, V.Le Taramelli 12, 27100, Pavia, Italy.
This review aims to provide the readership with an overview of the applications of the time-resolved spectroscopic techniques (often combined with steady-state measurements) in the elucidation of the mechanism of the photochemical behaviour of diaryl- and triarylamines. Such derivatives undergo cyclization to the carbazoles or ionization to the corresponding amine radical cations depending on both the nature of the starting substrates and the reaction conditions. In this context, time-resolved spectroscopy techniques allowed for the detection and the full characterization of all the excited states and the transients involved in these processes.
View Article and Find Full Text PDFOrg Lett
November 2024
School of Chemistry, College of Science, University of Tehran, 14155-6455 Tehran, Iran.
Here we report a simultaneous construction of two C-C and two C-N bonds in a unified procedure that incorporates alkynoic acid trifunctionalization, ortho C-H functionalization, and amination cascade. In an ordered process, the regioselective alkyne insertion reaction is favored over the decarboxylation process. The presence of the carboxyl group in alkynoic acid ensures the high regioselectivity in the carbopalladation process, paving the way for a novel method to synthesize unsymmetrically 2,3-diaryl substituted indole scaffolds with excellent regioselectivity.
View Article and Find Full Text PDFArch Biochem Biophys
November 2024
Department of Biochemistry, Faculty of Pharmacy, Anadolu University, Eskişehir, 26470, Turkey.
Sulfonamides, recognized as carbonic anhydrase (CA, EC 4.2.1.
View Article and Find Full Text PDFJ Org Chem
October 2024
State Key Laboratory of Chemical Resource Engineering, Department of Organic Chemistry, College of Chemistry, Beijing University of Chemical Technology, Beijing 100029, People's Republic of China.
Various -1,2,4-trihydrobenzo[][1,2]azaphosphinine 3-oxides are synthesized highly stereoselectively from generated phosphenes and formaldimines under microwave irradiation. Aryl(diazo)methyl(diaryl)phosphine oxides first undergo the Wolff rearrangement to generate phosphenes. Imines, generated from 1,3,5-triazinanes or paraformaldehyde and primary amines, nucleophilically attack the phosphenes followed by a tandem stereoelectronic effect-controlled intramolecular nucleophilic addition and aromatization to give final -1,2,4-trihydrobenzo[][1,2]azaphosphinine 3-oxides, exhibiting completely different annuloselectivity from linear nonformaldimines.
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